TÜV SÜD America Inc. will be participating in the 2010 MD&M West Trade Show at the Anaheim Convention Center, at booth #1876.

This year's conference will provide educational content for medical R&D, design, engineering, and quality professionals. Other highlights include: presentations from medical device companies, and information sessions on a variety of topics.

TÜV SÜD America Inc. provides IEC 60601-1-2/European Norm EN 60601-1-2:2001 certification, and immunity and emissions testing for Medical Devices.  TÜV is a Notified Body for the Medical Devices, Active Implantable Medical Devices, and In Vitro Diagnostic Directives, and is an SCC-qualified ISO 13485 Registrar for the Canadian Medical Device Regulations.  Additional services include FDA services, NRTL certification, and CE Marking assistance.  For more information, visit www.TUVamerica.com.  

To schedule an appointment with a TÜV SÜD America representative, click here.